Evidence map›Paper›PMID 29594492›Full record

ArticleMikrochimica acta2017

Enzyme-free amplified detection of circulating microRNA by making use of DNA circuits, a DNAzyme, and a catalytic hairpin assembly.

Jie Luo, Yongjie Xu, Jian Huang, Shu Zhang, Qi Xu, Jun He

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Article in Mikrochimica acta, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jie LuoDepartment of Laboratory Medicine, The Second People's Hospital of Guizhou Province, Guiyang, 550002, China. 13511917799@163.com.
Yongjie XuDepartment of Laboratory Medicine, Guizhou Provincial People's Hospital, Guiyang, 550002, China.
Jian HuangDepartment of Laboratory Medicine, Zunyi Medical University, Zunyi, 563003, China.
Shu ZhangDepartment of Laboratory Medicine, The Second People's Hospital of Guizhou Province, Guiyang, 550002, China.
Qi XuDepartment of Laboratory Medicine, The Second People's Hospital of Guizhou Province, Guiyang, 550002, China.
Jun HeDepartment of Laboratory Medicine, The Second People's Hospital of Guizhou Province, Guiyang, 550002, China. luojie0511040108@126.com.

Funding

science and technology foundation of Guizhou provincial health and family planning commission gzwjkj2016-1-066
6 · The paper itself

Abstract

A homogeneous and enzyme-free fluorometric assay is described for the determination of microRNA-182. It is based on the use of DNA circuits and DNAzyme. The DNA circuits warrant strong signal amplification by virtue of catalytic hairpin assembly, a system that consists of two hairpin substrates. A part of the DNAzyme sequence is programmed to sequester into one of the two hairpin substrates. In the presence of target microRNA-182, the two hairpin substrates undergo catalytic assembling. This results in the formation of a DNA duplex and the release of the DNAzyme from the hairpin structure. Upon cyclic amplification, one target catalyzes the formation of Mg (II)-dependent DNAzymes. These bind to, and hydrolyze, the fluorescently labeled substrates for signal amplification and transduction. Based on nucleic acid programmability, this engineered assay has a limit of detection as low as 6.8 f. and a dynamic range that covers the 10 f. to10 nM microRNA-182 concentration range. Detection can be performed within 60 min. The assay is simple, rapid, homogenous, cost-effective, and enzyme-free. These features make the method an attractive tool in routine microRNA diagnosis and, conceivably, in point of care uses. Graphical abstract Schematic of a homogeneous and enzyme-free fluorometric assay for the determination of microRNA-182. It is based on the use of DNA circuits and DNAzymes. The DNA circuits warrant strong signal amplification by virtue of catalytic hairpin assembly that uses two hairpin substrates. The method represents an attractive tool for routine microRNA diagnosis and, conceivably, point of care uses.

Indexed as

Biosensing TechniquesCirculating MicroRNADNA, CatalyticDNA ProbesFluorescent DyesHumansLimit of DetectionNucleic Acid Amplification TechniquesSpectrometry, FluorescenceCirculating MicroRNADNA, CatalyticDNA ProbesFluorescent DyesArtificial enzymesCascade reactionFlexibilityIsothermal assayLiquid biopsiesPoint-of-care testingProgrammabilityRapidityRoutine detectionSelf-assembly

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.